{"title":"丝网印刷电极条中碳电极面积的扩大和参比电极电位的漂移。","authors":"Jihyeon Kim,Seonhwa Park,Eunji Tak,Haesik Yang","doi":"10.1021/acs.analchem.5c00785","DOIUrl":null,"url":null,"abstract":"Screen-printed electrode (SPE) strips are widely used for electrochemical detection owing to their low cost, ease of fabrication, and suitability for point-of-care testing. Their electrochemical performance must remain reproducible across multiple uses, varied solution conditions, and extended measurement times; however, relevant studies are rare. In this study, we demonstrate that the electrochemical behavior of SPEs is significantly influenced by (i) dynamic changes in the real electrode area of carbon SPEs (working electrodes) and (ii) potential drifts in Ag SPEs (reference electrodes). The gradual wetting of pores in the carbon SPEs, which is affected by the solution composition and incubation time, increases the real electrode area and the non-Faradaic capacitive charging current. Notably, rapid wetting occurs in surfactant-containing and biological solutions. The wetting process also affects the Faradaic current of an electroactive species to a certain extent. Furthermore, the potential of Ag SPEs exhibits shifts with repeated use and under different incubation conditions, particularly in the presence of an electroactive species. These findings demonstrate that variations in the real electrode area and reference electrode potential play critical roles in SPE strip-based electrochemical measurements. Addressing these factors is essential for achieving accurate and reproducible results, particularly in repeated or long-term measurements, and in measurements involving surfactant-containing or biological solutions.","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"137 1","pages":""},"PeriodicalIF":6.7000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Expanding Carbon Electrode Area and Drifting Reference Electrode Potential in Screen-Printed Electrode Strips.\",\"authors\":\"Jihyeon Kim,Seonhwa Park,Eunji Tak,Haesik Yang\",\"doi\":\"10.1021/acs.analchem.5c00785\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Screen-printed electrode (SPE) strips are widely used for electrochemical detection owing to their low cost, ease of fabrication, and suitability for point-of-care testing. Their electrochemical performance must remain reproducible across multiple uses, varied solution conditions, and extended measurement times; however, relevant studies are rare. In this study, we demonstrate that the electrochemical behavior of SPEs is significantly influenced by (i) dynamic changes in the real electrode area of carbon SPEs (working electrodes) and (ii) potential drifts in Ag SPEs (reference electrodes). The gradual wetting of pores in the carbon SPEs, which is affected by the solution composition and incubation time, increases the real electrode area and the non-Faradaic capacitive charging current. Notably, rapid wetting occurs in surfactant-containing and biological solutions. The wetting process also affects the Faradaic current of an electroactive species to a certain extent. Furthermore, the potential of Ag SPEs exhibits shifts with repeated use and under different incubation conditions, particularly in the presence of an electroactive species. These findings demonstrate that variations in the real electrode area and reference electrode potential play critical roles in SPE strip-based electrochemical measurements. Addressing these factors is essential for achieving accurate and reproducible results, particularly in repeated or long-term measurements, and in measurements involving surfactant-containing or biological solutions.\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"137 1\",\"pages\":\"\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.analchem.5c00785\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.analchem.5c00785","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
摘要
丝网印刷电极(SPE)条由于其低成本、易于制造和适合于即时检测而广泛用于电化学检测。它们的电化学性能必须在多种用途、不同的溶液条件和延长的测量时间中保持可重复性;然而,相关的研究很少。在这项研究中,我们证明了spe的电化学行为受到(i)碳spe(工作电极)实际电极面积的动态变化和(ii) Ag spe(参考电极)的电位漂移的显著影响。受溶液组成和孵育时间的影响,碳SPEs的孔隙逐渐湿润,增加了实际电极面积和非法拉第电容充电电流。值得注意的是,在含表面活性剂和生物溶液中会发生快速润湿。润湿过程也在一定程度上影响电活性物质的法拉第电流。此外,Ag spe的电位在重复使用和不同的孵育条件下表现出变化,特别是在电活性物质存在的情况下。这些发现表明,真实电极面积和参考电极电位的变化在SPE条带电化学测量中起着至关重要的作用。解决这些因素对于获得准确和可重复的结果至关重要,特别是在重复或长期测量中,以及在涉及含有表面活性剂或生物溶液的测量中。
Expanding Carbon Electrode Area and Drifting Reference Electrode Potential in Screen-Printed Electrode Strips.
Screen-printed electrode (SPE) strips are widely used for electrochemical detection owing to their low cost, ease of fabrication, and suitability for point-of-care testing. Their electrochemical performance must remain reproducible across multiple uses, varied solution conditions, and extended measurement times; however, relevant studies are rare. In this study, we demonstrate that the electrochemical behavior of SPEs is significantly influenced by (i) dynamic changes in the real electrode area of carbon SPEs (working electrodes) and (ii) potential drifts in Ag SPEs (reference electrodes). The gradual wetting of pores in the carbon SPEs, which is affected by the solution composition and incubation time, increases the real electrode area and the non-Faradaic capacitive charging current. Notably, rapid wetting occurs in surfactant-containing and biological solutions. The wetting process also affects the Faradaic current of an electroactive species to a certain extent. Furthermore, the potential of Ag SPEs exhibits shifts with repeated use and under different incubation conditions, particularly in the presence of an electroactive species. These findings demonstrate that variations in the real electrode area and reference electrode potential play critical roles in SPE strip-based electrochemical measurements. Addressing these factors is essential for achieving accurate and reproducible results, particularly in repeated or long-term measurements, and in measurements involving surfactant-containing or biological solutions.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.